The invention relates to a closure system for containers used for storing or administering substances in the form of liquids, pastes or powders, which system is composed of a cap, provided with a through-hole, and of a closure element, said cap holding the closure element with a force fit and/or form fit on the container, in the area of the opening that is to be closed, by means of an undercut present on the container.
Aluminum caps for dental vials are known from DIN ISO 11 040 part 3 of year 1993. These caps are used to securely close glass cylinders, for example, by means of piston plugs or sealing discs. For this purpose, after the piston plugs or sealing discs have been applied, the caps are fixed on the glass cylinder by means of a deformation process carried out on the cap. Part 2 of the standard describes, among other things, thin sealing discs made of an elastomeric material.
The present invention provides a closure system for containers used for storing or administering substances in the form of liquids, pastes or powders, which system in one embodiment includes a cap, provided with a through-hole, and a closure element, wherein the cap holds the closure element with a force fit and/or form fit on the container, in the area of the container opening that is to be closed, by means of a catch element present on the container. For this purpose, the end face which surrounds the container opening, and on which the closure element bears, comprises a depression. The closure element is a virus-proof, bacteria-proof and spore-proof film that lies on the end face and, at least in some areas, over the depression. The cap is then fitted in place, an elastomer ring or adhesive ring is arranged between the closure element and the depression and fills the depression. With the present invention, a closure system for containers is provided that allows the container to be securely closed permanently and in a virus-proof, bacteria-proof and spore-proof manner.
The invention provides a closure system for containers which, without application of thermal energy, and in a mechanically simple way, allows the container to be securely closed permanently in a virus-proof, bacteria-proof and spore-proof manner.
In one of the preferred embodiments of the present invention, the end face which surrounds the container opening, and on which the closure element bears, comprises a depression. The closure element is a virus-proof, bacteria-proof and spore-proof film that lies on the end face and, at least in some areas, over the depression. When the cap is fitted in place, an elastomer ring or adhesive ring is arranged between the closure element and the depression and fills the depression.
In another embodiment of the invention, the closure element bears on an end face provided with an elevation. In this case, an elastomer ring is arranged on the closure element, and the elevation presses into this elastomer ring when the cap is fitted in place.
In yet another embodiment of the invention, a closure system is provided in which the cap, on its inner face directed towards the closure element, has at least one closed, elastic sealing lip that bears resiliently on the closure element.
In yet still another embodiment of the present invention, a closure system is provided without a cap. In this case, the elastomer ring, connected fixedly to the closure element, is clamped radially on a radial outer contour of the container, for example situated in the area of the opening that is to be closed.
The invention provides a closure system for containers which is easy and safe to handle and with which substances in the form of liquids, pastes or powders, in particular medicaments, for example pharmaceutical liquids containing proteins, are permanently enclosed in a sealed manner in a container.
Further details of the invention will become clear from the following illustrative embodiments which are depicted schematically in the Figures, in which:
The medicament chamber (10) is, in combination with the piston (40), an assembly group of an injection system. The medicament to be administered is initially stored, for example in liquid form, in the medicament chamber (10). For this purpose, the medicament has to be enclosed in the cylinder (11) of the chamber (10) in a virus-proof, bacteria-proof and spore-proof manner. The for example conical cylinder (11) has two openings (12, 13). A front opening (13) is the outlet nozzle. A rear opening (12) is used, inter alia, for filling the cylinder (11). When the chamber (10) is filled, the piston (40) is positioned in the rear area of the cylinder (11). Situated directly behind the piston (40), there is a cap (81) which, with the aid of a closure element (60), closes the rear opening (12) in a virus-proof, bacteria-proof and spore-proof manner. Of course, the container (10) can also be provided with just one opening (12), namely the opening (12) that is closed by the proposed closure system. If appropriate, the closure system can also be gas-tight.
For fixing the elastic cap (81), the rear area of the chamber (10), made from cyclo-olefin-copolymer (COC) plastic for example, has a defined contour (see
A further housing collar (31) is situated in the transition area between the end face (21) and the cylindrical outer contour (28). The width of this housing collar (31) is, for example, 50% of the wall thickness of the endpiece (20). The depth of this housing collar (31) is slightly greater than its width. The radial flank (32) of the housing collar (31) is cylindrical, while the axial flank (34) is flat.
Situated below the housing collar (31), there is a circumferential catch elevation (37), for example with two flanks. Its length corresponds to approximately 50% of the endpiece (20) length and is located between the two housing collars (31, 35). In this illustrative embodiment, the circumferential catch elevation (37), which is situated centrally there for example, is without interruption. The catch elevation (37) has a front flank (38) and a rear flank (39). The rear flank angle is, for example, 17±3 angular degrees, while the front flank angle is, for example, 51±3 angular degrees. The catch elevation (37) is rounded in the area of the zone of contact of the two flanks (38, 39).
According to
The cap (81) is made up of two portions, namely a securing area (91) and a base area (95). The securing area (91) is a substantially cylindrical tube-shaped portion and includes undercut (92) for contacting flank (38) of catch elevation (37) and cylindrical outer contour (28). It engages around the endpiece (20) in the area of the catch elevation (37) provided on the latter. Its inner contour is shaped exactly in such a way that, after the cap (81) has been fitted in place, it sits free of play on the endpiece (20), at least in the area of the flank (38). The inner contour does not bear on the other flank (39), or it bears on the latter in some areas only.
The base area (95), which according to
After the medicament chamber (10) has been filled and the piston (40) has been inserted, the sealing film (60), together with the elastomer ring (71), is fitted onto the end face (21) of the chamber (10). The elastomer ring (71) adhering to the sealing film (60) engages centrally around the radial flank (32) of the housing collar (31). When the cap (81) is fitted in place, it slides with its undercut (92) over the catch elevation (37). As soon as the undercut (92) bears on the front flank (38), the cap (81) has reached its end position. The base surface (96) then bears firmly on the sealing film (60). At the same time, the elastomer ring (71) in the area of the housing collar (31) sits sealingly between the cap (81) and the endpiece (20). In the axial direction, the elastomer ring (71) is forced in between the axial flank (34) and the sealing film (60) pressed firmly onto the base surface (96). The clamping force of the cap (81) is here generated, for example, by means of the annular clamping force of the securing area (91).
The housing collar (35) serves as an auxiliary abutment when the cap (81) is being fitted in place.
In small containers in particular, it is also conceivable for the cap to engage round the entire container. In this case, the cap then locks on the base of the container acting as catch element (37).
A further variant of
If appropriate, in this variant, an adhesive can be introduced into the annular channel (25) instead of an elastomer ring (72). This adhesive then bonds the applied sealing film (60) to the chamber (10).
Instead of a medicament chamber (10), it is also possible to use a glass vial (50) (see
In the vial (50), as also in the medicament chamber (10), the end face (21) can be designed sloping down towards the outside. Accordingly, the end face (21) describes a truncated cone for example, with a cone angle of 158±4 angular degrees for example. The imaginary cone tip lies outside the vial (50) or outside the medicament chamber (10).
The second, inner sealing lip (88) sits in a protected position under the first sealing lip (87). It presses the outer edge area of the sealing film (60) against the end face (21). It too is inclined by approximately 45 angular degrees relative to the sealing film (60). Both sealing lips (87, 88) are made of a permanently elastic material.
To ensure that the sealing film (60) can be placed at least more or less centrally on the end face (21) when assembling the closure system, this variant includes an abutment edge (22) whose height corresponds to at least twice the film thickness of the sealing film (60).
When the cap (84) is fitted in place, the inner sealing lip (88) presses the sealing film (60) into the channel (23). In doing so, the sealing film (60) is made taut, such that it lies flat.
If appropriate, the front area (89) of the sealing lip (88) can also point outwards. In this case, the front area is part of a cone surface, the tip of which lies above the upper surface (61) of the sealing film (60) on the continued centre line of the chamber (10). Here, for example, the channel (23) can be omitted.
The sealing film (60) bears on the end face (21) via the elastomer ring (73) that is arranged fixedly on it. The elastomer ring (73) has the shape of a perforated disc. In the compressed state in which it is installed, its material thickness is at least 30% greater than the height of the elevation (27). The elastomer ring (73) here reaches as far as the wall of the cylinder (11). In this variant, the clamping force of the cap (81) is determined by the elasticity of the elastomer ring (73).
The radial flank can in this case have a cylindrical contour (32) or a non-cylindrical contour (33). In
According to
Solutions are also possible in which the variants from
The sealing films (60) and if appropriate also the elastomer rings (71-73) can of course have self adhesive virus-proof coatings in the areas where they touch the end face (21) and the depressions (24, 25) or elevations (27).
Number | Date | Country | Kind |
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10 2006 040 888 | Aug 2006 | DE | national |
This is a continuation-in-part application of pending international application PCT/EP2007/007211 filed Aug. 16, 2007 and claiming the priority of German Application No. 10 2006 040 888.8 filed Aug. 31, 2006.
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90 11 309 | Oct 1990 | DE |
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Number | Date | Country | |
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20090159553 A1 | Jun 2009 | US |
Number | Date | Country | |
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Parent | PCT/EP2007/007211 | Aug 2007 | US |
Child | 12283231 | US |